These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

355 related articles for article (PubMed ID: 25951829)

  • 41. Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues.
    Begemann M; Spengler S; Kanber D; Haake A; Baudis M; Leisten I; Binder G; Markus S; Rupprecht T; Segerer H; Fricke-Otto S; Mühlenberg R; Siebert R; Buiting K; Eggermann T
    Clin Genet; 2011 Jul; 80(1):83-8. PubMed ID: 20738330
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Clinical Application of Sequential Epigenetic Analysis for Diagnosis of Silver-Russell Syndrome.
    Kim SY; Shin CH; Lee YA; Shin CH; Yang SW; Cho TJ; Ko JM
    Ann Lab Med; 2021 Jul; 41(4):401-408. PubMed ID: 33536359
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Silver-Russell syndrome in Hong Kong.
    Luk HM; Yeung KS; Wong WL; Chung BH; Tong TM; Lo IF
    Hong Kong Med J; 2016 Dec; 22(6):526-33. PubMed ID: 27468965
    [TBL] [Abstract][Full Text] [Related]  

  • 44. upd(20)mat is a rare cause of the Silver-Russell-syndrome-like phenotype: Two unrelated cases and screening of large cohorts.
    Hjortshøj TD; Sørensen AR; Yusibova M; Hansen BM; Dunø M; Balslev-Harder M; Grønskov K; van Hagen JM; Polstra AM; Eggermann T; Finken MJJ; Tümer Z
    Clin Genet; 2020 Jun; 97(6):902-907. PubMed ID: 32087029
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Exhaustive methylation analysis revealed uneven profiles of methylation at IGF2/ICR1/H19 11p15 loci in Russell Silver syndrome.
    Azzi S; Steunou V; Tost J; Rossignol S; Thibaud N; Das Neves C; Le Jule M; Habib WA; Blaise A; Koudou Y; Busato F; Le Bouc Y; Netchine I
    J Med Genet; 2015 Jan; 52(1):53-60. PubMed ID: 25395389
    [TBL] [Abstract][Full Text] [Related]  

  • 46. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
    Russo S; Calzari L; Mussa A; Mainini E; Cassina M; Di Candia S; Clementi M; Guzzetti S; Tabano S; Miozzo M; Sirchia S; Finelli P; Prontera P; Maitz S; Sorge G; Calcagno A; Maghnie M; Divizia MT; Melis D; Manfredini E; Ferrero GB; Pecile V; Larizza L
    Clin Epigenetics; 2016; 8():23. PubMed ID: 26933465
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Clinical and Molecular Heterogeneity of Silver-Russell Syndrome and Therapeutic Challenges: A Systematic Review.
    Singh A; Pajni K; Panigrahi I; Khetarpal P
    Curr Pediatr Rev; 2023; 19(2):157-168. PubMed ID: 35293298
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Quantitative analysis of methylation status at 11p15 and 7q21 for the genetic diagnosis of Beckwith-Wiedemann syndrome and Silver-Russell syndrome.
    Lee BH; Kim GH; Oh TJ; Kim JH; Lee JJ; Choi SH; Lee JY; Kim JM; Choi IH; Kim YM; Choi JH; Yoo HW
    J Hum Genet; 2013 Sep; 58(9):604-10. PubMed ID: 23803580
    [TBL] [Abstract][Full Text] [Related]  

  • 49. IGF-II serum levels are normal in children with Silver-Russell syndrome who frequently carry epimutations at the IGF2 locus.
    Binder G; Seidel AK; Weber K; Haase M; Wollmann HA; Ranke MB; Eggermann T
    J Clin Endocrinol Metab; 2006 Nov; 91(11):4709-12. PubMed ID: 16940449
    [TBL] [Abstract][Full Text] [Related]  

  • 50. A ten-year observation of somatic development of a first group of Polish children with Silver-Russell syndrome.
    Sienko M; Petriczko E; Zajaczek S; Zygmunt-Gorska A; Starzyk J; Korpysz A; Petriczko J; Walczak A; Walczak M
    Neuro Endocrinol Lett; 2014; 35(4):306-13. PubMed ID: 25038594
    [TBL] [Abstract][Full Text] [Related]  

  • 51. The Frequency of Methylation Abnormalities Among Estonian Patients Selected by Clinical Diagnostic Scoring Systems for Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome.
    Vals MA; Yakoreva M; Kahre T; Mee P; Muru K; Joost K; Teek R; Soellner L; Eggermann T; Õunap K
    Genet Test Mol Biomarkers; 2015 Dec; 19(12):684-91. PubMed ID: 26505556
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A boy with Silver-Russell syndrome and Sotos syndrome.
    Schwaibold EMC; Beygo J; Obeid K; Jauch A; Hinderhofer K; Moog U
    Am J Med Genet A; 2021 Feb; 185(2):549-554. PubMed ID: 33191647
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Screening of patients born small for gestational age with the Silver-Russell syndrome phenotype for DLK1 variants.
    Pham A; Sobrier ML; Giabicani E; Le Jules Fernandes M; Mitanchez D; Brioude F; Netchine I
    Eur J Hum Genet; 2021 Dec; 29(12):1756-1761. PubMed ID: 34276055
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Further heterogeneity in Silver-Russell syndrome: PLAG1 deletion in association with a complex chromosomal rearrangement.
    Brereton RE; Nickerson SL; Woodward KJ; Edwards T; Sivamoorthy S; Ramos Vasques Walters F; Chabros V; Marchin V; Grumball T; Kennedy D; Uzaraga J; Peverall J; Arscott G; Beilby J; Choong CS; Townshend S; Azmanov DN
    Am J Med Genet A; 2021 Oct; 185(10):3136-3145. PubMed ID: 34223693
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Russell-Silver syndrome.
    Eggermann T
    Am J Med Genet C Semin Med Genet; 2010 Aug; 154C(3):355-64. PubMed ID: 20803658
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Molecular and clinical studies in 138 Japanese patients with Silver-Russell syndrome.
    Fuke T; Mizuno S; Nagai T; Hasegawa T; Horikawa R; Miyoshi Y; Muroya K; Kondoh T; Numakura C; Sato S; Nakabayashi K; Tayama C; Hata K; Sano S; Matsubara K; Kagami M; Yamazawa K; Ogata T
    PLoS One; 2013; 8(3):e60105. PubMed ID: 23533668
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Cognitive Profiles and Brain Volume Are Affected in Patients with Silver-Russell Syndrome.
    Patti G; De Mori L; Tortora D; Severino M; Calevo M; Russo S; Napoli F; Confalonieri L; Schiavone M; Thiabat HF; Casalini E; Morana G; Rossi A; Ramenghi LA; Maghnie M; Di Iorgi N
    J Clin Endocrinol Metab; 2020 Apr; 105(4):. PubMed ID: 31665337
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Screening for genomic variants in ZFP57 in Silver-Russell syndrome patients with 11p15 epimutations.
    Spengler S; Gogiel M; Schönherr N; Binder G; Eggermann T
    Eur J Med Genet; 2009; 52(6):415-6. PubMed ID: 19632365
    [TBL] [Abstract][Full Text] [Related]  

  • 59. First report on concordant monozygotic twins with Silver-Russell syndrome and ICR1 hypomethylation.
    Riess A; Binder G; Ziegler J; Begemann M; Soellner L; Eggermann T
    Eur J Med Genet; 2016 Jan; 59(1):1-4. PubMed ID: 26691664
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Epigenetic and genetic diagnosis of Silver-Russell syndrome.
    Eggermann T; Spengler S; Gogiel M; Begemann M; Elbracht M
    Expert Rev Mol Diagn; 2012 Jun; 12(5):459-71. PubMed ID: 22702363
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.